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NeoPATH Pro-Tect HRP Detection Kit

FDA UDI

Class I (US FDA UDI)

by Biocare Medical, Llc

Identity

Trade Name
NeoPATH Pro-Tect HRP Detection Kit FDA UDI
Generic Name
Immunohistochemistry antibody detection IVD, kit, enzyme immunohistochemistry FDA UDI
Model / Reference
NPRI10031T135 FDA UDI

Identifiers

Primary DI / UDI-DI
00847627040817 FDA UDI
FDA Product Code
PPM FDA UDI
GMDN Term
Immunohistochemistry antibody detection IVD, kit, enzyme immunohistochemistry FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.4010 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Immunohistochemistry antibody detection IVD, kit, enzyme immunohistochemistry

NeoPATH Pro-Tect HRP Detection Kit by Biocare Medical, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Immunohistochemistry antibody detection IVD, kit, enzyme immunohistochemistry.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Biocare Medical, Llc

Sources (1)

  • FDA UDI 43ddcce0-94f0-4a48-8733-33f6cec56147 33 fields · synced Jun 8, 2026